FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

CONELOG Titanium base CAD/CAM

K Number: K143337 · Decision Feb 17, 2015
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
14
Review Days
89

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Basic Information

Device Name
CONELOG Titanium base CAD/CAM
K Number
K143337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Altatec GmbH
Date Received
November 20, 2014
Decision Date
February 17, 2015
Product Code
NHA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NHA Abutment, Implant, Dental, Endosseous

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Other Clearances by Altatec GmbH

K Number Device Name
K193401 Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants
K160784 CAM Titanium Blanks
K153779 Abutment for Bridges
K152509 CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)
K151599 iSy Implant System
K133991 ISY
K113779 CONELOG IMPLANT SYSTEM
K103252 CAMLOG VARIO SR ABUTMENTS
K090347 CAMLOG ABUTMENTS PS
K083496 CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS
Search all 14 clearances from Altatec GmbH →